chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170262264170262265CCA23GENIChomozygous60940238
1170262755170262756CT49GENIChomozygous60940239
1170262801170262802AC57GENIChomozygous60940240
1170263138170263139TA42GENIChomozygous60940241
1170263253170263254AG48GENIChomozygous60940242
1170263343170263344CT55GENIChomozygous60940243
1170263352170263353GA55GENIChomozygous60940244
1170264133170264134AG46GENIChomozygous60940245
1170264186170264187AG30GENIChomozygous60940246
1170264222170264223GGGTTT32GENIChomozygous60940247
1170264757170264758CT39GENIChomozygous60940248
1170264761170264762TC44GENIChomozygous60940249
1170265057170265058GA28GENIChomozygous60940250
1170266926170266927GC62GENIChomozygous60940251
1170267007170267008CT54GENIChomozygous60940252
1170267037170267038GA46GENIChomozygous60940253
1170267149170267150TC39GENICpossibly homozygous60940254
1170267150170267151TTCA29GENICpossibly homozygous60940255
1170267323170267324TC41GENIChomozygous60940256
1170267579170267580GA42GENIChomozygous60940257
1170267593170267594TC36GENIChomozygous60940258
1170267958170267959TC32GENIChomozygous60940259
1170268248170268249GT54GENICpossibly homozygous60940260
1170268395170268396CT34GENIChomozygous60940261
1170269050170269051AC58GENIChomozygous60940262
1170269357170269358AG24GENIChomozygous60940263
1170269412170269413AG19GENIChomozygous60940264
1170270085170270087GT--11GENICheterozygous60940265
1170270303170270304GA25GENIChomozygous60940266
1170270337170270338GA30GENIChomozygous60940267
1170271046170271047AG26GENIChomozygous60940268
1170271167170271168TC41GENIChomozygous60940269
1170271631170271632GA44GENIChomozygous60940270
1170271934170271935AG26GENIChomozygous60940271
1170272091170272102AAAAAAAAAAA-----------19GENIChomozygous60940272
1170272207170272208CT49GENIChomozygous60940273